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    Diet-Induced Developmental Acceleration Independent of TOR and Insulin in C. elegans

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    Authors
    MacNeil, Lesley T.
    Watson, Emma
    Arda, H. Efsun
    Zhu, Lihua Julie
    Walhout, Albertha J. M.
    UMass Chan Affiliations
    Program in Gene Function and Expression
    Program in Molecular Medicine
    Program in Systems Biology
    Document Type
    Journal Article
    Publication Date
    2013-03-28
    Keywords
    Caenorhabditis elegans
    Caenorhabditis elegans Proteins
    Insulin
    Gene Expression Regulation, Developmental
    Diet
    Biochemical Phenomena, Metabolism, and Nutrition
    Cell and Developmental Biology
    Genetics and Genomics
    Systems Biology
    
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    Link to Full Text
    http://dx.doi.org/10.1016/j.cell.2013.02.049
    Abstract
    Dietary composition has major effects on physiology. Here, we show that developmental rate, reproduction, and lifespan are altered in C. elegans fed Comamonas DA1877 relative to those fed a standard E. coli OP50 diet. We identify a set of genes that change in expression in response to this diet and use the promoter of one of these (acdh-1) as a dietary sensor. Remarkably, the effects on transcription and development occur even when Comamonas DA1877 is diluted with another diet, suggesting that Comamonas DA1877 generates a signal that is sensed by the nematode. Surprisingly, the developmental effect is independent from TOR and insulin signaling. Rather, Comamonas DA1877 affects cyclic gene expression during molting, likely through the nuclear hormone receptor NHR-23. Altogether, our findings indicate that different bacteria elicit various responses via distinct mechanisms, which has implications for diseases such as obesity and the interactions between the human microbiome and intestinal cells.
    Source
    Cell. 2013 Mar 28;153(1):240-52. doi: 10.1016/j.cell.2013.02.049. Link to article on publisher's website

    DOI
    10.1016/j.cell.2013.02.049
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/49906
    PubMed ID
    23540701
    Related Resources
    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.cell.2013.02.049
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